Linked Data
ClinVar Variation Id:
3132418
ClinVar RCV Id:
RCV004421346
dbSNP Id:
rs765019311
ExAC:
20:3063362 C / T
gnomAD v2:
20-3063362-C-T
gnomAD v4:
20-3082716-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3082716C>T , CM000682.2:g.3082716C>T | GRCh38 |
| NC_000020.10:g.3063362C>T , CM000682.1:g.3063362C>T | GRCh37 |
| NC_000020.9:g.3011362C>T | NCBI36 |
| NG_008663.1:g.7009G>A , LRG_715:g.7009G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.409G>A MANE Select | ENSP00000369647.3:p.Gly137Arg | |
| NM_000490.4:c.409G>A , LRG_715t1:c.409G>A | NP_000481.2:p.Gly137Arg | |
| XM_011529267.1:c.409G>A | XP_011527569.1:p.Gly137Arg | |
| XM_011529267.2:c.409G>A | XP_011527569.1:p.Gly137Arg | |
| NM_000490.5:c.409G>A MANE Select | NP_000481.2:p.Gly137Arg |